Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA5089257
Max Phase: Preclinical
Molecular Formula: C25H24N4O4S2
Molecular Weight: 508.63
Molecule Type: Unknown
Associated Items:
ID: ALA5089257
Max Phase: Preclinical
Molecular Formula: C25H24N4O4S2
Molecular Weight: 508.63
Molecule Type: Unknown
Associated Items:
Canonical SMILES: CC(=O)N1CCc2c(sc3nc(SCC(=O)Nc4cccc(C)c4)n(Cc4ccco4)c(=O)c23)C1
Standard InChI: InChI=1S/C25H24N4O4S2/c1-15-5-3-6-17(11-15)26-21(31)14-34-25-27-23-22(24(32)29(25)12-18-7-4-10-33-18)19-8-9-28(16(2)30)13-20(19)35-23/h3-7,10-11H,8-9,12-14H2,1-2H3,(H,26,31)
Standard InChI Key: PQMQUKJGFYOHJZ-UHFFFAOYSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
Molecule Type: Unknown | Topical: No | First In Class: No | Black Box: No |
Chirality: No | Availability: No | Prodrug: No |
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Molecular Weight: 508.63 | Molecular Weight (Monoisotopic): 508.1239 | AlogP: 4.04 | #Rotatable Bonds: 6 |
Polar Surface Area: 97.44 | Molecular Species: NEUTRAL | HBA: 8 | HBD: 1 |
#RO5 Violations: 1 | HBA (Lipinski): 8 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: 13.66 | CX Basic pKa: 2.19 | CX LogP: 3.56 | CX LogD: 3.56 |
Aromatic Rings: 4 | Heavy Atoms: 35 | QED Weighted: 0.31 | Np Likeness Score: -2.77 |
1. Carrasco K, Montersino C, Derviaux C, Saez-Ayala M, Hoffer L, Restouin A, Castellano R, Casassa J, Roche P, Pasquier E, Combes S, Morelli X, Collette Y, Betzi S.. (2022) CRCM5484: A BET-BDII Selective Compound with Differential Anti-leukemic Drug Modulation., 65 (7.0): [PMID:35348328] [10.1021/acs.jmedchem.1c02168] |
Source(1):